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HRID 76471作成日:2026年10月24日

1,4-Benzodioxan-6-ylamine → N2,N4-bis(3,4-ethylenedioxyphenyl)-5-fluoro-2,4-pyrimidinediamine

https://huagongshe.com/ja/reaction/76471

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-Benzodioxan-6-ylamineHCID 89148—
反応物2,4-Dichloro-5-fluoropyrimidineHCID 250705—
生成物N2,N4-bis(3,4-ethylenedioxyphenyl)-5-fluoro-2,4-pyrimidinediamineHCID 11596383—

反応手順

In like manner to the preparation of N2,N4-bis(3-hydroxyphenyl)-5-fluoro-2,4-pyrimidinediamine, 2,4-dichloro-5-fluoropyrimidine and 3,4-ethylenedioxyaniline were reacted to yield N2,N4-bis(3,4-ethylenedioxyphenyl)-5-fluoro-2,4-pyrimidinediamine. 1H NMR (CDCl3): δ 7.88 (d, 1H, J=3.6 Hz), 7.23 (d, 1H, J=2.3 Hz), 7.15 (d, 1H, J=2.4 Hz), 7.00 (dd, 1H, J=3 and 8.1 Hz), 6.98 (dd, 1H, J=3 and 8 Hz), 6.83 (d, 1H, J=8.7 Hz), 6.81 (d, 1H, J=8.7 Hz), 6.7 (s, 1H), 6.58 (s, 1H), 4.23 (m, 4H), 4.24 (m, 4H); 19F NMR (CDCl3): δ−47445; LCMS: ret. time: 21.81 min.; purity: 96%; MS (m/e): 397 (MH|).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835430B2
出典データセットuspto-grants-2014_09
ORD IDord-29d09617d9bb4cbfb299e43fe6a58897
出典メモuspto-grants-2014_09